Overview
Evaluation of Gastrointestinal Transit Pre and Pos Treatment With Non Selective Betablocker in a Population of Cirrhotics
Status:
Unknown status
Unknown status
Trial end date:
2021-05-01
2021-05-01
Target enrollment:
0
0
Participant gender:
All
All
Summary
The purpose of this study is to evaluate the influence of non betablockers in gastrointestinal motility (transit time) in patients with liver cirrhosis.Phase:
N/AAccepts Healthy Volunteers?
NoDetails
Lead Sponsor:
ALDO TORRE DELGADILLOTreatments:
Adrenergic beta-Antagonists
Propranolol
Criteria
Inclusion Criteria:- Cirrhosis of any ethiology
- Child Pugh A, B, C without beta-blocker treatment previously (min. 1 month without
treatment)
- Patients with previous variceal bleeding (with liver cirrhosis) * Patients with
ascites or bacterial spontaneous peritonitis
Exclusion Criteria:
- Variceal disease without cirrhosis
- Cirrhotics patients that use antibiotics, prebiotics and probiotics during the study
period and one month previously
- Patients under immunosuppressor treatment
- Patients with portal thrombosis
- Patients with Sd. Budd-Chiari or cava/suprahepatic thrombosis
- Patients with active infection process